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FADS2 c.744+1920T>A
Variant ID: 11-61617676-T-A
NM_004265.3(
FADS2
):c.744+1920T>A
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Deciphering regulatory DNA sequences and noncoding genetic variants using neural network models of massively parallel reporter assays.
Plos One
Movva, Rajiv R; Greenside, Peyton P; Marinov, Georgi K GK; Nair, Surag S; Shrikumar, Avanti A; Kundaje, Anshul A
Publication Date: 2019
Variant appearance in text: rs174591
PubMed Link:
31206543
Variant Present in the following documents:
Main text
pone.0218073.pdf
View BVdb publication page
Low LDL cholesterol, PCSK9 and HMGCR genetic variation, and risk of Alzheimer's disease and Parkinson's disease: Mendelian randomisation study.
Bmj (Clinical Research Ed.)
Benn, Marianne M; Nordestgaard, Børge G BG; Frikke-Schmidt, Ruth R; Tybjærg-Hansen, Anne A
Publication Date: 2017-04-24
Variant appearance in text: rs174591
PubMed Link:
28438747
Variant Present in the following documents:
benm033277.ww1.pdf
View BVdb publication page